Basic information Safety Supplier Related

3-(1,3-OXAZOL-5-YL)ANILINE

Basic information Safety Supplier Related

3-(1,3-OXAZOL-5-YL)ANILINE Basic information

Product Name:
3-(1,3-OXAZOL-5-YL)ANILINE
Synonyms:
  • 5-(3-AMINOPHENYL)OXAZOLE
  • 3-(1,3-OXAZOL-5-YL)ANILINE
  • BUTTPARK 43\57-51
  • 3-(oxazol-5-yl)benzenaMine
  • 3-(5-Oxazolyl)aniline
  • [3-(1,3-Oxazol-5-yl)phenyl]amine
  • [3-(Oxazol-5-yl)phenyl]amine
  • 3-(5-Oxazolyl)benzenamine
CAS:
157837-31-5
MF:
C9H8N2O
MW:
160.17
Product Categories:
  • Amines
  • Phenyls & Phenyl-Het
  • API intermediates
  • Phenyls & Phenyl-Het
  • Amines and Anilines
  • Heterocycles
Mol File:
157837-31-5.mol
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3-(1,3-OXAZOL-5-YL)ANILINE Chemical Properties

Melting point:
93-95°C
Boiling point:
359.1±25.0 °C(Predicted)
Density 
1.204
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.81±0.10(Predicted)
form 
solid
Appearance
Light brown to brown Solid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-36-22
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2921420090
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3-(1,3-OXAZOL-5-YL)ANILINE Usage And Synthesis

Synthesis

89808-77-5

157837-31-5

General procedure for the synthesis of 3-(5-oxazolyl)aniline using 5-(3-nitrophenyl)oxazole as starting material: firstly, intermediate 1a (3.52 g, 18.5 mmol) was dissolved in anhydrous ethanol (210 ml), followed by addition of water (21 ml) for dilution. Next, SnCl2-2H2O (20.9 g, 92.6 mmol) and HCl (15 ml, 180 mmol) were added to the reaction system. After the reaction mixture was stirred overnight at room temperature, the pH was adjusted using 10% NaOH aqueous solution to 7. Subsequently, the reaction mixture was extracted several times with EtOAc. The organic phases were combined, dried with MgSO4, filtered and the solvent was evaporated to give 3-(5-oxazolyl)aniline in the form of a light orange powder (2.74 g, 93% yield). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6) with chemical shifts of δ8.37 (s, 1H), 7.49 (s, 1H), 7.10 (t, J=7.8 Hz, 1H), 6.90 (t, J=1.8 Hz, 1H), 6.86 (d, J=7.6 Hz, 1H), 6.59-6.54 ( m, 1H), 5.25 (s, 2H).

References

[1] Patent: WO2015/144614, 2015, A1. Location in patent: Page/Page column 32; 33
[2] Patent: EP3144307, 2017, A1. Location in patent: Paragraph 0085; 0087
[3] Patent: WO2007/60026, 2007, A1. Location in patent: Page/Page column 53-54
[4] Patent: EP1612204, 2006, A1. Location in patent: Page/Page column 22

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